211043-68-4

Basic information

• Product Name: ((4R,5S)-2-oxo-4,5-diphenyloxazolidin-3-yl)acetic acid
• Synonyms: ((4R,5S)-2-oxo-4,5-diphenyloxazolidin-3-yl)acetic acid
• CAS NO: 211043-68-4
• Molecular Weight: 297.31
• Mol File: 211043-68-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: ((4R,5S)-2-oxo-4,5-diphenyloxazolidin-3-yl)acetic acid(CAS DataBase Reference)
• NIST Chemistry Reference: ((4R,5S)-2-oxo-4,5-diphenyloxazolidin-3-yl)acetic acid(211043-68-4)
• EPA Substance Registry System: ((4R,5S)-2-oxo-4,5-diphenyloxazolidin-3-yl)acetic acid(211043-68-4)

Safety Data

• Hazardous Substances Data: 211043-68-4(Hazardous Substances Data)

Upstream product

• 86286-50-2 (4R,5S)-4,5-diphenyl-1,3-oxazolidin-2-one 
• 211043-74-2 ethyl ((4R,5S)-2-oxo-4,5-diphenyloxazolidin-3-yl)acetate 

Relevant articles and documents

Application of erythro-2-amino-1,2-diphenylethanol as a highly efficient chiral auxiliary. highly stereoselective staudinger-type β-lactam synthesis using a 2-chloro-l-methylpyridinium salt as the dehydrating agent

The Staudinger-type reaction of carboxylic acids with imines, using a 2-chloro-l-methylpyridinium salt as the dehydrating reagent, proceeded smoothly under mild conditions to afford the desired β-lactams in high yields with excellent cis-selectivity. This